Conserved Genetic Interactions between Ciliopathy Complexes Cooperatively Support Ciliogenesis and Ciliary Signaling

Mutations in genes encoding cilia proteins cause human ciliopathies, diverse disorders affecting many tissues. Individual genes can be linked to ciliopathies with dramatically different phenotypes, suggesting that genetic modifiers may participate in their pathogenesis. The ciliary transition zone c...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:PLoS Genet
Egile Nagusiak: Yee, Laura E., Garcia-Gonzalo, Francesc R., Bowie, Rachel V., Li, Chunmei, Kennedy, Julie K., Ashrafi, Kaveh, Blacque, Oliver E., Leroux, Michel R., Reiter, Jeremy F.
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Public Library of Science 2015
Gaiak:
Research Article
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC4635004/
https://ncbi.nlm.nih.gov/pubmed/26540106
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pgen.1005627
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